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  4. Synthesis of beta -amino-alpha -hydroxy esters and beta -amino-alpha -azido ester by Sharpless asymmetric aminohydroxylation, byproducts analysis
 
research article

Synthesis of beta -amino-alpha -hydroxy esters and beta -amino-alpha -azido ester by Sharpless asymmetric aminohydroxylation, byproducts analysis

Liu, Zuosheng
•
Ma, Nianchun
•
Jia, Yanxing
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2005
The Journal of Organic Chemistry

Synthesis of enantiomerically pure beta -amino-alpha -hydroxy esters, e.g., I, and beta -amino-alpha -azido ester using Sharpless AA as a key step is described. A side reaction, the oxidn. of the beta -hydroxy-alpha -amino ester into the alpha ,alpha -di-tert-butyloxycarbamoyl-beta -ketoester under AA conditions, is also documented. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1021/jo047772o
Author(s)
Liu, Zuosheng
Ma, Nianchun
Jia, Yanxing
Bois-Choussy, Michele
Malabarba, Adriano
Zhu, Jieping  
Date Issued

2005

Published in
The Journal of Organic Chemistry
Volume

70

Issue

7

Start page

2847

End page

2850

Subjects

Esters Role: SPN (Synthetic preparation)

•

PREP (Preparation) (amino; stereoselective prepn. of amino hydroxy esters via Sharpless asym. aminohydroxylation of diisopropoxy(methoxy)cinnamate with t-Bu carbamate); Asymmetric synthesis and induction (stereoselective prepn. of amino hydroxy esters via Sharpless asym. aminohydroxylation of diisopropoxy(methoxy)cinnamate with t-Bu carbamate); Aminohydroxylation (stereoselective

•

Sharpless; stereoselective prepn. of amino hydroxy esters via Sharpless asym. aminohydroxylation of diisopropoxy(methoxy)cinnamate with t-Bu carbamate)

•

cinnamate Sharpless aminohydroxylation; amino hydroxy ester asym prepn; azido amino ester asym prepn

Note

CAN 142:410947

23-17

Aliphatic Compounds

Institut de Chimie des Substances Naturelles,CNRS,Gif-sur-Yvette,Fr.

Journal

written in English.

171738-31-1P; 482627-91-8P Role: BYP (Byproduct), PREP (Preparation) (byproducts from the stereoselective prepn. of amino hydroxy esters via Sharpless asym. aminohydroxylation of diisopropoxy(methoxy)cinnamate with t-Bu carbamate); 850404-78-3P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of (Boc-amino)azido[diisopropoxy(methoxy)phenyl]propanoate via mesylation of (Boc-amino)hydroxy[diisopropoxy(methoxy)phenyl]propanoate followed by azidation); 863301-53-5P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of (Boc-amino)hydroxy[diisopropoxy(methoxy)phenyl]propanoate via mesylation of (Boc-amino)hydroxy[diisopropoxy(methoxy)phenyl]propanoate followed by substitution); 850404-79-4P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of (Boc-amino)hydroxy[diisopropoxy(methoxy)phenyl]propanoate via mesylation of (Boc-amino)hydroxy[diisopropoxy(methoxy)phenyl]propanoate followed by substitution); 850404-75-0P Role: BYP (Byproduct), SPN (Synthetic preparation), PREP (Preparation) (prepn. of aryldi(Boc-amino)oxopropanoates via Sharpless aminohydroxylation of aryl(Boc-amino)hydroxypropanoates); 136620-75-2 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of aryldi(Boc-amino)oxopropanoates via Sharpless aminohydroxylation of aryl(Boc-amino)hydroxypropanoates); 850404-76-1P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of aryldi(Boc-amino)oxopropanoates via Sharpless aminohydroxylation of aryl(Boc-amino)hydroxypropanoates); 850404-77-2P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of(Boc-amino)azido[diisopropoxy(methoxy)phenyl]propanoate via mesylation of (Boc-amino)hydroxy[diisopropoxy(methoxy)phenyl]propanoate followed by azidation); 4248-19-5 (tert-Butyl carbamate); 850404-72-7 Role: RCT (Reactant), RACT (Reactant or reagent) (stereoselective prepn. of amino hydroxy esters via Sharpless asym. aminohydroxylation of diisopropoxy(methoxy)cinnamate with t-Bu carbamate); 850404-73-8P; 850404-74-9P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (stereoselective prepn. of amino hydroxy esters via Sharpless asym. aminohydroxylation of diisopropoxy(methoxy)cinnamate with t-Bu carbamate)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58462
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